QuickView for RNF168 (gene)

Gene Symbol:

RNF168 Homo sapiens

Full name:

ring finger protein 168

Synonyms:

hRNF168, E3 ubiquitin-protein ligase RNF168, RING-type E3 ubiquitin transferase RNF168, ring finger protein 168, E3 ubiquitin protein ligase

Genomic Location:

Chr 3: 197683025-197714979

Description:

This gene encodes an E3 ubiquitin ligase protein that contains a RING finger, a motif present in a variety of functionally distinct proteins and known to be involved in protein-DNA and protein-protein interactions. The protein is involved in DNA double-strand break (DSB) repair. Mutations in this gene result in Riddle syndrome.

This gene encodes an E3 ubiquitin ligase protein that contains a RING finger, a motif present in a variety of functionally distinct proteins and known to be involved in protein-DNA and protein-protein interactions. The protein is involved in DNA double-strand break (DSB) repair. Mutations in this gene result in Riddle syndrome.

View Less

Orthologs:

Mus musculus ,  Rattus norvegicus ,  Macaca mulatta ,  Danio rerio ,  Canis lupus familiaris ,  Bos taurus ,  Pan troglodytes ,  Gallus gallus

External Links:

Entrez Gene

Transcription Factor
Binding Sites:

GGGCGGR_SP1_Q6 ,  GGCNRNWCTTYS_UNKNOWN ,  GCGNNANTTCC_UNKNOWN ,  SCGGAAGY_ELK1_02

Cytogenetic Map:

3q29

search → result